ABSTRACT
Sections of 565 radicular cysts were examined for keratinization of epithelium. 4 cysts showed keratinization, 2 of ortho and 2 of para type. Due to other histological features typical for odontogenic keratocysts, it was concluded that these cysts were odontogenic keratocysts that occurred in the periapical region of the involved teeth.
Subject(s)
Odontogenic Cysts/pathology , Periapical Diseases/pathology , Radicular Cyst/pathology , Epithelium/pathology , Humans , KeratinsSubject(s)
Bone Resorption/complications , Carcinoma/diagnosis , Hypercalcemia/complications , Osteolysis/complications , Osteoporosis/complications , Pancreatic Neoplasms/diagnosis , Carcinoma/complications , Humans , Lymphatic Metastasis , Male , Middle Aged , Pancreatic Neoplasms/complications , SkullSubject(s)
Crohn Disease/drug therapy , Metronidazole/therapeutic use , Adult , Female , Humans , Male , Middle AgedABSTRACT
Prenatal detection of "Cri du chat" syndrome, as the consequence of balanced translocation 46,XY,t (5, 15) (p 13, p11) of the father, is described. A phenotipically normal child, with the same type of translocation possesed by his father was born in this family, as well as a child with "Cri du chat" syndrome. Four pregnancies were termed by spontaneous abortion. In the seventh pregnancy amniocenthesis was performed. On the basis of cell culture of amniotic fluid the diagnosis of "Cri du chat" syndrome was established. The diagnosis was confirmed by culture of peripheral blood of prematurely born foetus. Tissue cultures of some fetal organs were performed in order to find the origin of amniotic cells whose culture served for screening cytogenetic analysis.